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Jan Fischer

Showing results (51-60 of 66) with videos related to

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EMBO Reports|September 13, 2022
Human-specific ARHGAP11B ensures human-like basal progenitor levels in hominid cerebral organoidsJan Fischer, Eduardo Fernández Ortuño, Fabio Marsoner, et al.
The Journal of Biological Chemistry|June 30, 2016
Gingipains of Porphyromonas gingivalis Affect the Stability and Function of Serine Protease Inhibitor of Kazal-type 6 (SPINK6), a Tissue Inhibitor of Human KallikreinsKarolina Plaza, Magdalena Kalinska, Oliwia Bochenska, et al.
Biochemical and Biophysical Research Communications|February 2, 2016
The solution structure of the kallikrein-related peptidases inhibitor SPINK6Sascha Jung, Jan Fischer, Björn Spudy, et al.
The Journal of Investigative Dermatology|December 20, 2013
Characterization of Spink6 in mouse skin: the conserved inhibitor of kallikrein-related peptidases is reduced by barrier injuryJan Fischer, Zhihong Wu, Tomasz Kantyka, et al.
Parkinsonism & Related Disorders|February 11, 2025
Variable expressivity of KMT2B variants at codon 2565 in patients with dystonia and developmental disordersAntonia M Stehr, Jan Fischer, Nazanin Mirza-Schreiber, et al.
Parkinsonism & Related Disorders|March 22, 2025
Corrigendum to "Variable expressivity of KMT2B variants at codon 2565 in patients with dystonia and developmental disorders" [Parkinson. Relat. Disord. (2025) 133 107319]Antonia M Stehr, Jan Fischer, Nazanin Mirza-Schreiber, et al.
Clinical Genetics|July 30, 2022
The recurrent TCF4 missense variant p.(Arg389Cys) causes a neurodevelopmental disorder overlapping with but not typical for Pitt-Hopkins syndromeBernt Popp, Thierry Bienvenu, Irina Giurgea, et al.
Virology|May 29, 2004
An amino-terminal segment of hantavirus nucleocapsid protein presented on hepatitis B virus core particles induces a strong and highly cross-reactive antibody response in miceAstrid Geldmacher, Dace Skrastina, Ivars Petrovskis, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 20, 2023
De novo PHF5A variants are associated with craniofacial abnormalities, developmental delay, and hypospadiasFrederike L Harms, Alexander J M Dingemans, Maja Hempel, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 9, 2023
De novo PHF5A variants are associated with craniofacial abnormalities, developmental delay, and hypospadiasFrederike L Harms, Alexander J M Dingemans, Maja Hempel, et al.
Pageof 7

Showing results (51-60 of 66) with videos related to

Sort By:
Pageof 7
EMBO Reports|September 13, 2022
Human-specific ARHGAP11B ensures human-like basal progenitor levels in hominid cerebral organoidsJan Fischer, Eduardo Fernández Ortuño, Fabio Marsoner, et al.
The Journal of Biological Chemistry|June 30, 2016
Gingipains of Porphyromonas gingivalis Affect the Stability and Function of Serine Protease Inhibitor of Kazal-type 6 (SPINK6), a Tissue Inhibitor of Human KallikreinsKarolina Plaza, Magdalena Kalinska, Oliwia Bochenska, et al.
Biochemical and Biophysical Research Communications|February 2, 2016
The solution structure of the kallikrein-related peptidases inhibitor SPINK6Sascha Jung, Jan Fischer, Björn Spudy, et al.
The Journal of Investigative Dermatology|December 20, 2013
Characterization of Spink6 in mouse skin: the conserved inhibitor of kallikrein-related peptidases is reduced by barrier injuryJan Fischer, Zhihong Wu, Tomasz Kantyka, et al.
Parkinsonism & Related Disorders|February 11, 2025
Variable expressivity of KMT2B variants at codon 2565 in patients with dystonia and developmental disordersAntonia M Stehr, Jan Fischer, Nazanin Mirza-Schreiber, et al.
Parkinsonism & Related Disorders|March 22, 2025
Corrigendum to "Variable expressivity of KMT2B variants at codon 2565 in patients with dystonia and developmental disorders" [Parkinson. Relat. Disord. (2025) 133 107319]Antonia M Stehr, Jan Fischer, Nazanin Mirza-Schreiber, et al.
Clinical Genetics|July 30, 2022
The recurrent TCF4 missense variant p.(Arg389Cys) causes a neurodevelopmental disorder overlapping with but not typical for Pitt-Hopkins syndromeBernt Popp, Thierry Bienvenu, Irina Giurgea, et al.
Virology|May 29, 2004
An amino-terminal segment of hantavirus nucleocapsid protein presented on hepatitis B virus core particles induces a strong and highly cross-reactive antibody response in miceAstrid Geldmacher, Dace Skrastina, Ivars Petrovskis, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 20, 2023
De novo PHF5A variants are associated with craniofacial abnormalities, developmental delay, and hypospadiasFrederike L Harms, Alexander J M Dingemans, Maja Hempel, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 9, 2023
De novo PHF5A variants are associated with craniofacial abnormalities, developmental delay, and hypospadiasFrederike L Harms, Alexander J M Dingemans, Maja Hempel, et al.
Pageof 7